Compound Identification
SMILES
CC1=C2C(O[C@@H]3O[C@H](CO[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@@H](O)[C@H](O)[C@H]3O)=CC(=O)OC2=CC=C1
InChIKey
InChIKey=LGVTTZBZMYKZOR-NYKIBTIESA-N
Formula
C22H28O13
Mass
500.453
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Phenylpropanoids and polyketides
-
Class
Coumarins and derivatives
- Subclass Coumarin glycosides
-
Class
Coumarins and derivatives
-
Superclass
Phenylpropanoids and polyketides
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Coumarins and derivatives
Subclass
Coumarin glycosides
Intermediate Tree Nodes
Not available
Direct Parent
Coumarin glycosides
Alternative Parents
O-glycosyl compounds Disaccharides 1-benzopyrans Pyranones and derivatives Oxanes Benzenoids Vinylogous esters Heteroaromatic compounds Secondary alcohols Lactones Polyols Oxacyclic compounds Acetals Hydrocarbon derivatives Organic oxides Primary alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Coumarin-4-o-glycoside - Coumarin o-glycoside - Disaccharide - Glycosyl compound - O-glycosyl compound - Benzopyran - 1-benzopyran - Pyranone - Oxane - Benzenoid - Pyran - Heteroaromatic compound - Vinylogous ester - Lactone - Secondary alcohol - Polyol - Organoheterocyclic compound - Oxacycle - Acetal - Alcohol - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Primary alcohol - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as coumarin glycosides. These are aromatic compounds containing a carbohydrate moiety glycosidically bound to a coumarin moiety.
External Descriptors
Not available